Latest Medical Affairs Partner - Nephrology & R Jobs

Labelling Strategy and Development, Oncology Team Lead

Lead a global team responsible for developing and managing oncology product labels, ensuring regulatory compliance and alignment with patient care and commercial goals. Drive strategic labelling governance, engage with regulatory authorities, and collaborate with cross-functional R&D teams to shape innovative, patient-focused labelling solutions.

GSK

Hybrid Permanent

Labelling Strategy and Development, Oncology Team Lead

Leads a global team responsible for developing and managing oncology product labeling strategies across the R&D lifecycle. This role ensures regulatory compliance, collaborates with cross-functional stakeholders, and shapes patient-focused labeling standards while advising senior leadership and engaging with regulatory authorities to drive innovation in labeling practices.

GSK United States

Hybrid Permanent

Associate Director, Biostatistics

The role involves leading statistical strategy and execution across clinical development programs, including study design, data analysis, and regulatory submissions. The individual will provide expert statistical input, manage internal or outsourced programming teams, and represent biostatistics in interactions with global regulatory agencies. Emphasis is placed on innovation, cross-functional collaboration, and delivery of high-quality statistical outputs for clinical trials and submissions.

CSL

Hybrid Permanent

Associate Director, Biostatistics

This role leads the statistical strategy and execution for clinical development programs within a therapeutic area, ensuring robust study design, data analysis, and regulatory compliance. The Associate Director collaborates with cross-functional teams, represents biostatistics in regulatory interactions, and oversees internal or outsourced programming efforts. They also drive innovation in statistical methodologies and contribute to clinical trial interpretation and reporting.

CSL

Hybrid Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing, executing, and interpreting clinical studies, creating development plans, and collaborating with cross-functional teams to ensure regulatory submissions and product approvals globally. The role also includes providing expert input on trial design, regulatory activities, and engaging with external stakeholders to drive strategic insights.

Pfizer US$214,900 – US$358,100 pa

On-site Permanent

Global Development Lead, Internal Medicine, Sr. Director (non-MD)

The Global Development Lead (GDL) is responsible for leading the clinical development of assigned assets in Internal Medicine. This involves designing and executing clinical trials, creating development plans, and ensuring regulatory compliance. The role also includes collaborating with cross-functional teams, providing expert input on clinical data, and engaging with external stakeholders to drive strategic insights.

Pfizer

On-site Permanent

Engineering Technician

The Engineering Technician role involves providing comprehensive engineering support for the Steriles Business Unit, focusing on equipment maintenance, GMP compliance, and continuous improvement initiatives. Responsibilities include breakdown repairs, calibration, quality documentation, and project support, all while maintaining high safety and regulatory standards.

GSK Barnard Castle, United Kingdom

On-site Permanent Shift-work

Head of RTSM (Randomization and Trial Supply Management)

This role involves leading the RTSM function, partnering with clinical development, operations, quality, and external vendors to design and deliver patient-focused randomization and clinical supply solutions. Responsibilities include managing cross-functional teams, ensuring on-time randomization and supply availability, and improving RTSM processes and governance.

GSK Stevenage, United Kingdom

Hybrid Permanent

Process Engineer

The Process Engineer role involves providing technical expertise to support safe and efficient manufacturing at GSK's Montrose site. Responsibilities include resolving technical issues, contributing to capital projects, improving process plant software, and collaborating with cross-functional teams to ensure compliance and process improvements.

GSK Montrose, Alba / Scotland, DD10 8JB, United Kingdom

On-site Contract

Operational Quality Director

The Operational Quality Director at GSK will lead the end-to-end quality oversight of manufacturing activities, ensuring compliance with GMP standards and regulatory requirements. Key responsibilities include managing batch documentation, overseeing real-time quality control, and leading the QP team to maintain high-quality standards and inspection readiness.

GSK East Hertfordshire, United Kingdom

On-site Permanent

Clinical Programmer/Analyst

The Clinical Programmer/Analyst designs, builds, and reviews programming solutions to transform clinical and real-world data into reliable results for regulatory and research purposes. Working closely with statisticians and data scientists, the role involves developing validated datasets, tables, listings, and figures using CDISC standards such as SDTM and ADaM, while ensuring compliance with GxP and ICH guidelines. The position supports agile delivery within a hybrid work environment and emphasizes technical excellence, collaboration, and innovation in clinical data programming.

GSK Stevenage, United Kingdom

Hybrid Permanent

NIS P&D Study Delivery Lead, Associate Director

The NIS P&D Study Delivery Lead, Associate Director, is responsible for leading the full lifecycle of clinical studies and trials within the Non-Interventional Study (NIS) portfolio. This includes designing, executing, and reporting complex regulatory commitment studies, managing team members, and ensuring compliance with regulatory guidelines. The role also involves leading operational decision-making, risk management, and driving innovation in study delivery through new technologies.

GSK Stevenage, United Kingdom £87,000 pa

Hybrid Permanent

NPI Launch Lead

This role leads the logistics and project management for new pharmaceutical and consumer product launches at GSK’s Barnard Castle site, ensuring timely, compliant market rollouts. The NPI Launch Lead coordinates cross-functional teams, manages launch timelines across global markets, and ensures adherence to GMP, quality, and regulatory standards throughout the product introduction lifecycle.

GSK Barnard Castle, United Kingdom

Hybrid Permanent

Process Technologist

As a Process Technologist, you will support the production area by providing technical services, troubleshooting, and working on technical projects. You will collaborate with cross-functional teams to ensure product quality and compliance, execute process validation, and perform root cause analysis for material and processing issues.

GSK Barnard Castle, United Kingdom

On-site Permanent

Laboratory Analyst

The Laboratory Analyst supports product testing and analysis within GMP-compliant laboratories at GSK’s Ware site, ensuring safe and effective oral and solid dose medicines are produced. The role involves sample preparation, analytical testing using methodologies like HPLC, and maintaining compliance with safety and quality standards. Collaboration with cross-functional teams is key to maintaining supply and driving continuous improvement in a fast-paced manufacturing environment.

GSK East Hertfordshire, United Kingdom

On-site Permanent